Recruiting

RISE & ECAU

Sponsor:

Boston University

Code:

NCT06906302

Conditions

Intimate Partner Violence (IPV)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

RISE

Advocacy-based ECAU

Study Details

Brief summary:

This study aims to improve treatment for Veterans Health Administration (VHA) patients who experience intimate partner violence (IPV). This study will evaluate two brief counseling interventions for VHA patients who have experienced IPV in the past 12 months: Recovering from IPV through Strength and Empowerment (RISE) and advocacy-based Enhanced Care as Usual (ECAU). The RISE intervention includes up to 8 sessions and includes specific topic areas (e.g., social support, health effects, resources). The other intervention, ECAU, includes a single session that includes supportive education about IPV and health effects, discussion of ways to increase safety, and information about resources. This study will test which approach is better for improving self-efficacy and other aspects of health.

Participants will answer surveys about their self-efficacy and other health and safety indicators (e.g., mental health symptoms) right before receiving treatment, approximately 12 weeks later, and then every three months after that for one year. Participation in this research will last about 15 months.

Conditions

Intimate Partner Violence (IPV)

Study ID

NCT06906302

Start date

Sep 15, 2025

Status verified date

Oct, 2025

Completion date

Jan, 2030

Anticipated

Primary completion date

Jan, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • patients receiving care at an enrolled site/affiliated Community-Based Outpatient Clinic (CBOC)
  • report experience of past-year physical, psychological, and/or sexual IPV on an established screening tool used to detect IPV in VHA, and
  • be able to provide informed consent including permission to have intervention sessions recorded

Exclusion Criteria:

  • severe cognitive impairment,
  • suicide or homicide intent with a specific plan
  • untreated or unstable symptoms of mania or psychosis

Study Design

Enrollment

172 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: RISE (Recovering from Intimate Partner Violence through Strengths and Empowerment)

Participants randomized to the RISE arm will have 1 or more RISE sessions.

active comparator: Advocacy-based ECAU (Enhanced Care as Usual)

Participants randomized to this arm will have a single Advocacy-based ECAU session

Interventions

RISE

RISE is personalized, trauma-informed, empowerment-oriented and variable-length, consisting of an initial 60-minute session and up to 7 additional 45-minute sessions (1-8 sessions total).

Advocacy-based ECAU

Advocacy-based ECAU is a single 60-minute trauma-informed counseling intervention that includes supportive education, validating and empathetic statements, safety planning, resource provision and referrals.

Primary outcome measure

  • Self-efficacy [ Time Frame: Baseline, 3 months, 6 months. 9 months, 12 months, 15 months ]

Central Contacts and Locations

Central contacts

Locations

VA Boston Healthcare System

Recruiting

Boston, Massachusetts, United States, 02130

VA Minneapolis Healthcare System

Recruiting

Minneapolis, Minnesota, United States, 55417

VA Philadelphia Healthcare System

Recruiting

Philadelphia, Pennsylvania, United States, 19104

More Information

Sponsor

Boston University

Last update posted

Oct 14, 2025

Last verified

Oct, 2025

Keywords

  • RISE
  • Enhanced Care as Usual (ECAU)
  • Healthcare patients
  • Self-efficacy
  • Depression
  • Post-Traumatic Stress Disorders (PTSD)

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Boston University on 2025-10-14.